Observational Epidemiological Studies Flashcards

1
Q

How would you work out point prevalence?

A

(number of persons with disease at some time point) / (total population at risk of disease at the same time point)

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2
Q

name 3 types of descriptive epidemiological studies

A

ecological studies
case reports / case series
cross-sectional studies

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3
Q

What 2 broad things do we need to do when we assess if association is causal?

A

1 - consider bias, confounding, and chance as possible explanations

2 - consider the criteria for causality

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4
Q

What 2 forms of bias might crop up in observed epidemiological studies?

A

selection bias

information bias

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5
Q

What is selection bias?

A

occurs when the way in which groups of subjects are selected for a study means that the groups cannot be validly compared with each other (or with the general population)

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6
Q

Name 4 examples of selection bias

A

sampling bias
response bias
healthy worker effect
healthy reproducer effect

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7
Q

What is information bias?

A

when the way in which the data are obtained from groups being compared differs systematically

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8
Q

Name 5 examples of information bias

A
recall bias
recording bias
interviewer bias
lost to follow up bias
social acceptability bias
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9
Q

How would you work out incidence rate?

A

(number of new cases) / (number of person-years accumulated)

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10
Q

How would you work out the risk?

A

(number of new cases) / (number of persons at risk at beginning of observation period)

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11
Q

name 3 key functions of descriptive studies

A

To alert the medical community to what types of persons were most / least affected by disease

To assist in the evidence-based planning of health and medical care facilities

To provide suggestions concerning disease aetiology for further investigation using analytic studies (hypothesis generation)

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12
Q

When would you use a cross-sectional study?

A

If in a particular geographical region we were to determine the point prevalence of a particular disease then a cross-sectional study is often undertaken
□ Determining need for specific health or social services
□ Development of hypotheses concerning risk factors for a disease

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13
Q

Name 2 advantages of cross-secitonal studies

A

cheap

quick

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14
Q

Name 3 disadvantages of cross-sectional studies

A

Time sequence and causation (disease and exposure measured simultaneously and so sometimes hard to interpret results in terms of cause and effect)

Cohort effects when interpreting relationships with age

Problems with interpretation of prevalence which is a mixutre of incidence and survival relating to disease

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15
Q

What is an ecological study?

A

Studies in which the units of observation are groups of individuals rather than individuals themselves, for example, populations of different countries, or town, or health regions / districts

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16
Q

What are the 2 main disadvantages of ecological studies?

A

The group of people described by disease data are often not the same people as those described by the exposure data

The time relationship between the measurements for exposure and disease is often unclear
(So we cannot assume from a relationship found amongst groups of individuals, that the same relationship also holds at the individual level)

17
Q

Name 3 advantages of Ecological studies

A

Quick
Inexpensive
Hypothesis generation

18
Q

What are cohort studies?

A

Cohort studies are studies in which a group of individuals who are defined on the basis of the exposure to a risk factor and are then followed up over time to determine who develops disease of interest

19
Q

What are the 2 types of cohort studies?

A

prospective

retrospective

20
Q

What are the 5 key advantages to cohort studies?

A

Provide estimates of absolute and cumulative risks of disease

Particularly useful for following up rare exposures

Eliminate some of the sources of bias which are unavoidable in case-control studies which rely on recall of past events i.e. if carefully conducted then recall bias is eliminated

Because exposure is measured before disease occurrence there is little doubt about cause and effect

Unlike case-control studies which address a single disease, there is no limit to the disease for which the risk of occurrence may be related to exposure

21
Q

What are the 3 key disadvantages to cohort studies?

A

Not useful for very rare diseases as few of the individuals exposed will develop the disease - but a case-control study design would be much more satisfactory

As they often involve following up large numbers of people over decades they are expensive and difficult to maintain, particularly from a funding stream perspective

If disease is rare and we only need relative risks associated with different levels of exposure to risk factors then unnecessarily expensive

22
Q

What might you use to choose the comparison cohort in a cohort study?

A

The general population and the use of SMRs and SIRs
National surveys
Another occupational group
Regional studies
A sub-cohort of the original exposed cohort

23
Q

How might you refine measurements of exposure?

A

Dichotomous (ever/never exposed)
Categorical (no/low/medium/high)
Quantitative measured exposure (continuous variable)

24
Q

What are the sources of measurement of exposure in a cohort study?

A

existing records
questionnaires to study subjects
clinical investigations

25
Q

What are the 2 main sources of bias in a cohort study?

A

healthy worker bias

lost to follow up bias

26
Q

What is the relative risk?

A

ratio between absolute risk in exposed and unexposed cohorts

27
Q

What is attributable risk?

A

different absolute risk in exposed and unexposed cohorts

28
Q

What is a case control study?

A

a group of individuals with a particular disease (the cases) are retrospectively compared with an appropriately selected group of controls in relation to their previous level of exposure to the risk factors of interest

29
Q

What is a nested study?

A

□ A study is nested (usually case-control studies) when it recruits study subjects from a population whose characteristics are known because its members are already the subjects of an existing larger study (for example, a cohort study or large RCT)

30
Q

What are the 3 main advantages to case control studies?

A

Effective use of resources to study the aetiological factors for rare diseases

Explore multiple exposures (risk factors) for a disease

Can estimate relative risk of disease associated with different levels of exposure to a risk factor through the odds-ration approximation to the relative risk

31
Q

What are the 3 main disadvantages to case control studies?

A

Recall bias e.g. abdo x ray in pregnant women and childhood cancer
People with cancer may remember things better

Address single disease only

Can’t absolute risks

32
Q

What are the steps of design with case control studies?

A
case definition
selection of controls
sources of controls
matching controls to cases
sources of bias
33
Q

where might you get controls for a case control study?

A
From the underlying cohort from which the cases were ascertained
Hospital controls
GP controls
Neighbourhood controls
Random digit dialing by telephone
34
Q

What are the main sources of bias in a case control study?

A
recall bias
recording bias
interviewer bias
response bias
sampling bias
35
Q

What problem is posed by case control studies in analysis and how is this navigated?

A

we don’t have incidence rate

there is an approximatino to the relative risk whihc can be estimated - the OR

36
Q

What does OR do?

A

is approximates RR which is better for rare disease

37
Q

How would you calculate OR?

A

(odds of disease in exposed group) / (odds of disease in unexposed group)

38
Q

What are the 9 Bradford criteria for assessing causality?

A
1 biological plausability
2 time
3 strength of association
4 biological gradient or dose-response relationship
5 consistency
6 specificity
7 coherence
8 experiments
9 analogy